Diagnostic imaging catheter

ABSTRACT

A diagnostic imaging catheter includes a drive shaft provided with a signal transmitting and receiving unit at a distal portion thereof and which is rotatable and movable forward and backward, a sheath into which the drive shaft is inserted, a relay connector coupled to a proximal end of the sheath, a support tube provided at an outer circumference of the drive shaft along an axial direction and which moves forward and backward in conjunction with the drive shaft, a seal member provided inside the relay connector and which seals a space between the relay connector and the support tube, and an injection opening located in a region closer to a distal side than the seal member and closer to a proximal side than a distal end of the support tube in a backward movement limit position thereof and via which a liquid is able to be injected into the sheath.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to Japanese Application No. 2016-101712filed on May 20, 2016, the entire content of which is incorporatedherein by reference.

TECHNICAL FIELD

The disclosure herein relates to a diagnostic imaging catheter.

BACKGROUND ART

Heretofore, as a medical device that is used to acquire a diagnosticimage to diagnose, for example, a lesion area in the living body, thereis a diagnostic imaging catheter that is used in an imaging apparatusfor diagnosis using, for example, intravascular ultrasound (IVUS) oroptical coherence tomography (OCT).

The diagnostic imaging catheter is equipped with a drive shaft, which isprovided with a transmitting and receiving unit that transmits andreceives inspection waves, and a sheath, into which the drive shaft isinserted in such a manner as to be movable forward and backward. Duringthe use of the diagnostic imaging catheter, what is called a pullbackoperation (an inward pulling operation) is performed which moves thedrive shaft from a distal side to a proximal side by moving the driveshaft backward while rotating the drive shaft, or a push-in operation isperformed which pushes the drive shaft into the distal side (refer toJapanese Patent Application Publication No. 2015-119994).

When the diagnostic imaging catheter is used, the inside of the sheathis filled with a priming liquid such as a physiological salt solution (apriming process) so as to efficiently transmit and receive inspectionwaves. To fill the inside of the sheath with the priming liquid, asyringe is usually connected to a port provided at a hub on the handside, and the priming liquid is injected into the sheath. Then, theinjected priming liquid flows toward the distal side through a gapbetween the sheath and the drive shaft and is thus discharged from acommunicating hole provided at the distal end of the sheath to theoutside of the catheter.

The pushing force necessary on the syringe to inject the priming liquiddepends on the flow path resistance in a flow path through which thepriming liquid flows. In other words, as the flow path resistance islarger, a larger pushing force is required on the syringe. Therefore, inorder to smoothly perform the priming process, it is desirable to reducethe flow path resistance. Here, the flow path resistance is inverselyproportionate to the diameter of the flow path through which the primingliquid flows and is proportionate to the length of the flow path throughwhich the priming liquid flows.

While examples of the method for reducing the flow path resistanceinclude increasing a gap (flow path diameter) between the sheath and thedrive shaft, increasing the gap may cause the vibration of thetransmitting and receiving unit occurring during the rotation of thedrive shaft to become large, so that an image may not be able to beappropriately acquired.

Based upon the above, a diagnostic imaging catheter is needed whichallows the priming process to be smoothly performed by reducing the flowpath resistance without increasing the gap between the sheath and thedrive shaft.

In relation to this, for example, Japanese Patent ApplicationPublication No. 2000-083959 discloses a diagnostic imaging catheter inwhich a priming port is provided at a unit connector (corresponding to asheath connector) provided at the distal side of a hub (corresponding toa drive shaft connector). According to the diagnostic imaging catheterdisclosed therein, since the length of a flow path through which apriming liquid flows is shorter than that in a diagnostic imagingcatheter in which the port is provided at the hub, the flow pathresistance can be reduced.

However, with respect to a diagnostic imaging catheter according toJapanese Patent Application Publication No. 2000-083959, in order tosmoothly perform a priming process, a further reduction of the flow pathresistance is demanded.

One consideration though, is that if the priming liquid directlycontacts the drive shaft during the priming process, the drive shaft maybe, for example, deformed or damaged, so that an image may not be ableto be appropriately acquired.

In view of the above-mentioned problems, the disclosure herein providesa diagnostic imaging catheter which allows a priming process to besmoothly performed by reducing the flow path resistance withoutincreasing a gap between the sheath and the drive shaft, whilepreventing a priming liquid from contacting the drive shaft to disableappropriately acquiring an image.

SUMMARY

A diagnostic imaging catheter according to an exemplary embodiment ofthe disclosure includes a drive shaft which is provided with a signaltransmitting and receiving unit at a distal portion thereof and which isrotatable and movable forward and backward, a sheath into which thedrive shaft is inserted, a relay connector which is coupled to aproximal end of the sheath, a support tube which is provided at an outercircumference of the drive shaft along an axial direction and whichmoves forward and backward in conjunction with the drive shaft, a sealmember which is provided inside the relay connector and which seals aspace between the relay connector and the support tube, and an injectionopening which is located in a region closer to a distal side than theseal member and closer to a proximal side than a distal end of thesupport tube in a backward movement limit position thereof and via whicha liquid is able to be injected into the sheath.

According to the diagnostic imaging catheter configured as describedabove, a priming liquid is injected via the injection opening, which islocated in the region closer to the distal side than the seal member,which is provided inside the relay connector. Therefore, the length ofthe flow path through which the priming liquid flows is short ascompared with a configuration in which a port is provided at a unitconnector or a hub, and the flow path resistance is thus reduced.Accordingly, the priming process can be smoothly performed by reducingthe flow path resistance without increasing the gap between the sheathand the drive shaft. Moreover, since the injection opening is locatedcloser to the proximal side than the distal end of the support tube inthe backward movement limit position thereof, when the priming liquid isinjected via the injection opening, the priming liquid contacts thesupport tube, which is provided at the outer circumference of the driveshaft. Therefore, the priming liquid can be prevented from contactingthe drive shaft to hinder appropriately acquiring an image.

With the above-described configuration, a diagnostic imaging cathetercan be provided which allows the priming process to be smoothlyperformed by reducing the flow path resistance without increasing a gapbetween the sheath and the drive shaft, while preventing the primingliquid from contacting the drive shaft and hindering appropriatelyacquiring an image.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a plan view illustrating a state in which an externalapparatus is connected to a diagnostic imaging catheter according to anexemplary embodiment of the disclosure.

FIGS. 2A and 2B are diagrams schematically illustrating the entireconfiguration of the diagnostic imaging catheter according to anexemplary embodiment of the disclosure, in which FIG. 2A is a side viewof the diagnostic imaging catheter before a pullback operation (aninward pulling operation) is performed and FIG. 2B is a side view of thediagnostic imaging catheter when the pullback operation is beingperformed.

FIG. 3 is an enlarged sectional view thereof illustrating aconfiguration of a distal side of the diagnostic imaging catheter.

FIG. 4 is an enlarged sectional view thereof illustrating aconfiguration of a portion near a relay connector in a state in which asupport tube is in a forward movement limit position.

FIG. 5 is an enlarged sectional view thereof illustrating aconfiguration of the portion near the relay connector in a state inwhich the support tube is in a backward movement limit position.

FIG. 6 is an enlarged sectional view thereof illustrating aconfiguration of a portion near a unit connector.

FIG. 7 is an enlarged sectional view thereof illustrating aconfiguration of a proximal side of the diagnostic imaging catheter.

FIG. 8 is a diagram schematically illustrating the entire configurationof a diagnostic imaging catheter according to a further exemplaryembodiment of the disclosure.

DETAILED DESCRIPTION

Hereinafter, embodiments of the disclosure will be described withreference to the accompanying drawings. Furthermore, the followingdescription should not be construed to limit the technical scope setforth in the claims or the meanings of terms. Moreover, dimensionalratios illustrated in the drawings are exaggerated for the purpose ofillustration and may be different from the actual ratios.

FIG. 1 is a plan view illustrating a state in which an externalapparatus 300 is connected to a diagnostic imaging catheter 100according to an exemplary embodiment of the disclosure, FIGS. 2A and 2Bare diagrams schematically illustrating the entire configuration of thediagnostic imaging catheter 100, FIG. 3 is a diagram illustrating aconfiguration of a distal side of the diagnostic imaging catheter 100,FIG. 4 and FIG. 5 are diagrams illustrating a configuration of a portionnear a relay connector 170, FIG. 6 is a diagram illustrating aconfiguration of a portion near a unit connector 150, and FIG. 7 is adiagram illustrating a configuration of a proximal side of thediagnostic imaging catheter 100.

The diagnostic imaging catheter 100 according to the exemplaryembodiment may be applied to intravascular ultrasound (IVUS). Asillustrated in FIG. 1, the diagnostic imaging catheter 100 is drivenwhile being connected to the external apparatus 300.

As illustrated in FIG. 1 and FIGS. 2A and 2B, the diagnostic imagingcatheter 100 includes, in broad terms, a sheath 110, which is insertedinto a body cavity in the living body, an outer tube 120, which isprovided at a proximal side of the sheath 110, an inner shaft 130, whichis inserted into the outer tube 120 in such a way as to be movableforward and backward, a drive shaft 140, which is equipped with atransducer unit 145 configured to transmit and receive signals at adistal end of the drive shaft 140, and which is provided in such a wayas to be rotatable and movable forward and backward inside the sheath110, a relay connector 170, which interconnects the sheath 110 and theouter tube 120, a support tube 180, which is provided on an outercircumference of the drive shaft 140 along an axial direction and whichmoves forward and backward in conjunction with the drive shaft 140, aunit connector 150, which is provided at a proximal side of the outertube 120 and which is configured to hold the inner shaft 130 inside, anda hub 160, which is provided on a proximal side of the inner shaft 130.

In the context of the disclosure, a side of the diagnostic imagingcatheter 100 which is inserted into a body cavity is referred to as adistal end or a distal side, a side of the diagnostic imaging catheter100 on which the hub 160 is provided is referred to as a proximal end ora proximal side, and an extending direction of the outer tube 120 isreferred to as an axial direction.

As illustrated in FIG. 2A, the drive shaft 140 extends up to the insideof the hub 160 through the sheath 110, the relay connector 170, thesupport tube 180, the outer tube 120, the inner shaft 130, and the unitconnector 150.

The hub 160, the inner shaft 130, the drive shaft 140, the transducerunit 145, and the support tube 180 are interconnected in such a way asto be integrally movable forward and backward in the axial direction.Therefore, when an operation to push the hub 160 toward the distal sideis performed, the inner shaft 130 connected to the hub 160 is pushedinto the outer tube 120 and the unit connector 150, the drive shaft 140and the transducer unit 145 are moved inside the sheath 110 toward thedistal side, and the support tube 180 is moved inside the relayconnector 170 toward the distal side. For example, when an operation topull the hub 160 toward the proximal side is performed, the inner shaft130 is pulled out of the outer tube 120 and the unit connector 150 asindicated by an arrow a1 in FIG. 1 and FIG. 2B, the drive shaft 140 andthe transducer unit 145 are moved inside the sheath 110 toward theproximal side as indicated by an arrow a2, and the support tube 180 ismoved inside the relay connector 170 toward the proximal side asindicated by an arrow a3.

As illustrated in FIG. 2A, when the inner shaft 130 is pushed toward thedistal side to a maximum extent, a distal portion of the inner shaft 130reaches the vicinity of the relay connector 170. At this time, thetransducer unit 145 is located in the vicinity of the distal end of thesheath 110.

As illustrated in FIG. 2B, a falling-out preventive protrusion 131 (seeFIG. 6) is provided at a distal end of the inner shaft 130. Thefalling-out preventive protrusion 131 has the function of preventing theinner shaft 130 from falling out of the outer tube 120. The falling-outpreventive protrusion 131 is configured to engage an inner wall 152B(see FIG. 6) of the unit connector 150 when the hub 160 is pulled towardthe proximal side to a maximum extent, in other words, when the innershaft 130 is pulled out of the outer tube 120 and the unit connector 150to a maximum extent. Moreover, even when the hub 160 is pulled towardthe proximal side to a maximum extent, the support tube 180 is locatedcloser to the distal side than an injection opening 173 a, which isdescribed below (see a position indicated by reference character B inFIG. 5).

As illustrated in FIG. 3, the drive shaft 140 includes a pipe body 140 ahaving flexibility, and a signal line 140 b which is inserted throughthe pipe body 140 a. The pipe body 140 a can be configured with, forexample, multiple layers of coils having different winding directionsaround the axis. Examples of the material of the coils include stainlesssteel and a nickel-titanium (Ni—Ti) alloy. The signal line 140 b can beconfigured with, for example, a twisted pair cable or a coaxial cable.

The transducer unit 145 includes an ultrasound transducer (correspondingto a signal transmitting and receiving unit) 145 a, which transmits andreceives ultrasound waves, and a housing 145 b, which contains theultrasound transducer 145 a.

The ultrasound transducer 145 a has the function of transmittingultrasound waves, which serve as inspection waves, into a body cavity,and receiving ultrasound waves reflected from the body cavity. Theultrasound transducer 145 a is electrically connected to an electrodeterminal 166 (see FIG. 7) via the signal line 140 b.

The ultrasound transducer 145 a can be made from a piezoelectricmaterial, such as ceramic or a crystal.

As illustrated in FIG. 3, the sheath 110 is equipped with a lumen 110 a,into which the drive shaft 140 is inserted in such a way as to bemovable forward and backward. A guide wire insertion member 114, whichis equipped with a guide wire lumen 114 a into which a guide wire W isable to be inserted, is attached to a distal portion of the sheath 110in such a way to be arranged in parallel with the lumen 110 a providedin the sheath 110. The sheath 110 and the guide wire insertion member114 can be configured in an integrated fashion with the use of, forexample, heat-welding. The guide wire insertion member 114 is providedwith a marker 115 having a radiopaque property. The marker 115 isconfigured with a metal coil having a high radiopaque property, such asPt, Au, or Ir.

A communicating hole 116, through which the inside of the lumen 110 acommunicates with the outside thereof, is formed at the distal portionof the sheath 110. Moreover, a reinforcement member 117, which is usedto rigidly join and support the guide wire insertion member 114, isprovided at the distal portion of the sheath 110. The reinforcementmember 117 is provided with a communicating passage 117 a, through whichthe communicating hole 116 communicates with the inside of the lumen 110a that is located closer to the proximal side than the reinforcementmember 117. Furthermore, the distal portion of the sheath 110 does notnecessarily need to be provided with the reinforcement member 117.

The communicating hole 116 is a priming liquid discharge hole throughwhich the priming liquid can be discharged. When using the diagnosticimaging catheter 100, the operator performs a priming process to fillthe inside of the sheath 110 with the priming liquid so as to reduce theattenuation of ultrasound waves caused by air inside the sheath 110 andto efficiently transmit and receive ultrasound waves. When the primingprocess is performed, the priming liquid is released to the outsidethrough the communicating hole 116, so that a gas such as air can bedischarged from the inside of the sheath 110 together with the primingliquid.

The sheath 110 is formed of a material having a high ultrasoundtransmissivity. In a preferred embodiment, the distal portion of thesheath 110, defined by the range of where the ultrasound transducer 145a can move in the axial direction of the sheath 110, forms an acousticwindow portion having ultrasound transmissivity higher than those ofother portions of the sheath 110.

The sheath 110, the guide wire insertion member 114, and thereinforcement member 117 are formed of a material having flexibility,and the material is not limited to a specific material. Examples of thematerial include various thermoplastic elastomers, such as a styreneelastomer, a polyolefin elastomer, a polyurethane elastomer, a polyesterelastomer, a polyamide elastomer, a polyimide elastomer, a polybutadieneelastomer, a trans-polyisoprene elastomer, a fluororubber elastomer, anda chlorinated polyethylene elastomer. A combination of one or two ormore (polymer alloy, polymer blend, or laminated body) of theseelastomers can also be used as the material. Furthermore, a hydrophiliclubricant coating layer which exhibits lubricating ability at the timeof wetting can be arranged on the outer surface of the sheath 110.

As illustrated in FIG. 4 and FIG. 5, the relay connector 170interconnects the sheath 110 and the outer tube 120. The relay connector170 includes an outer tube holding portion 171, which is provided on theproximal side, an anti-kink protector 172, which is provided on thedistal side, and a port 173, which communicates with the injectionopening 173 a through which a priming liquid is able to be injected. Therelay connector 170 is equipped with a lumen 170 a, into which the driveshaft 140 and the support tube 180 are inserted in such a way as to bemovable forward and backward.

The outer tube holding portion 171 is inserted into the anti-kinkprotector 172 at the distal side and is fixed in such a manner that aconvex portion 171A, which is provided on the outer circumference of theouter tube holding portion 171, is fitted in a concave portion 172A,which is provided on the inner circumference of the anti-kink protector172. Thus, the outer tube holding portion 171 is fixedly connected tothe anti-kink protector 172.

A bearing 174, which supports the drive shaft 140 and the support tube180, is provided on the inside of the outer tube holding portion 171.The outer tube holding portion 171 holds the outer tube 120 incooperation with the bearing 174.

Moreover, an X-ring (corresponding to a seal member) 175, which seals aspace between the outer tube holding portion 171 and the support tube180, is provided on the inside of the outer tube holding portion 171 andon the distal side of the bearing 174. Therefore, when the primingliquid is injected, the priming liquid can be prevented from flowingtoward the proximal side between the outer tube holding portion 171 andthe support tube 180. The configuration for sealing a space between theouter tube holding portion 171 and the support tube 180 is not limitedto the illustrated X-ring, but can be, for example, an O-ring. Thematerial used to configure the outer tube holding portion 171 caninclude a relatively hard resin material.

The anti-kink protector 172 is mounted for the purpose of smoothing avariance in hardness at a connection portion between the sheath 110 andthe outer tube holding portion 171, which differ greatly in hardness.Therefore, it is desirable that the anti-kink protector 172 be formed ofa material having a hardness lower than that of the outer tube holdingportion 171. In this way, providing the anti-kink protector 172 enablespreventing, for example, bends and kinks of the sheath 110 in a portionat which the sheath 110 is exposed from the outer tube holding portion171. Furthermore, while, in the exemplary embodiment, the anti-kinkprotector 172 is configured as a member separate from the outer tubeholding portion 171, the configuration is not specifically limiting andthe anti-kink protector 172 can be configured integrally with the outertube holding portion 171 and configured in a spiral cut shape.

As illustrated in FIG. 4, when the support tube 180 is located in aforward movement limit position (see a position indicated by referencecharacter A in FIG. 4), the sheath 110, the drive shaft 140, and thesupport tube 180 are in a state of being pulled out of the inside of theanti-kink protector 172 toward the distal side. Moreover, as illustratedin FIG. 5, when the support tube 180 is located in a backward movementlimit position (see a position indicated by reference character B inFIG. 5), the sheath 110 and the drive shaft 140 are in a state of beingpulled out of the inside of the anti-kink protector 172 toward theproximal side.

As illustrated in FIG. 4 and FIG. 5, the port 173 is configuredintegrally with the outer tube holding portion 171. According to thisconfiguration, since the port 173 is made from a relatively hardmaterial, the port 173 is unlikely to deform when the syringe S isconnected thereto, as compared with a case where a port is configuredintegrally with an anti-kink protector. The port 173 communicates withthe injection opening 173 a, and the injection opening 173 acommunicates with the lumen 170 a. When the priming process isperformed, the syringe S (see FIG. 1) is connected to the port 173.

In this way, since the injection opening 173 a is provided at the relayconnector 170, the port 173 is provided at a position closer to thedistal side than in a configuration in which a port for priming isprovided, for example, at a hub or a unit connector as in the prior art.Accordingly, the length of the flow path through which the primingliquid flows up to the communicating hole 116 is small so as to reducethe flow path resistance and to enable smoothly performing the primingprocess, so that a burden on the operator can be decreased. Moreover,the length of the flow path through which the priming liquid flows up tothe communicating hole 116 being small enables decreasing the injectedamount of the priming liquid. Therefore, since the amount of actionrequired by the operator to push the syringe S when injecting thepriming liquid is decreased, the priming process can be smoothlyperformed and, thus, a burden on the operator can be decreased.

Furthermore, a plurality of protrusions or step differences D (see FIG.6 and FIG. 7) is configured in a lumen leading from the hub 160 to therelay connector 170. The step difference D illustrated in FIG. 6 isconfigured for the purpose of causing the falling-out preventiveprotrusion 131 to be engaged and stop there, and the step difference Dillustrated in FIG. 7 is configured for the purpose of receiving andholding the inner shaft 130. For example, in the case of a configurationin which a port for priming is provided at a hub, when the primingliquid passes the step difference D, a whirlpool may occur to cause airbubbles. Then, when the air bubbles together with the priming liquidmoves to the distal side of the sheath 110 and attaches to thetransducer unit 145 (air trap), the propagation of ultrasound is blockedand a signal measured by the transducer unit 145 becomes weak, so thatan image may not be able to be appropriately acquired. However, in thecase of the diagnostic imaging catheter 100 according to the exemplaryembodiment herein, since the port 173 is provided at the relay connector170, such a phenomenon that the priming liquid passes the stepdifference D and flows toward the distal side does not occur.Accordingly, the occurrence of such an air trap as mentioned above canbe adequately prevented.

Moreover, for example, in the case of a configuration in which the portis provided at a hub, a protrusion is required to be provided at the hubso as to determine the direction of the hub when the hub is connected tothe external apparatus 300. On the other hand, in the case of thediagnostic imaging catheter 100 according to the exemplary embodimentherein, since the injection opening 173 a is provided at the relayconnector 170, the above-mentioned protrusion is not required.

The port 173 is configured to be inclined from the directionperpendicular to the axial direction toward the proximal side, asillustrated in FIG. 4. This configuration, when the priming liquid isinjected, enables the priming liquid to flow toward the distal sidethrough the injection opening 173 a, as compared with a configuration inwhich a port is provided along the direction perpendicular to the axialdirection. Therefore, the force with which the operator pushes thesyringe S can be decreased.

The injection opening 173 a is located on the distal side of the X-ring175 and closer to the proximal side than the center 170 c of the relayconnector 170 in the axial direction. According to this configuration,the injection opening 173 a is configured in the vicinity of the X-ring175. Therefore, air trapped between the injection opening 173 a and theX-ring 175 can be reduced.

As illustrated in FIG. 4 to FIG. 6, the support tube 180 is provided onthe outer circumference of the drive shaft 140 and the innercircumference of the relay connector 170 along the axial direction, thuscovering and protecting the drive shaft 140.

As illustrated in FIG. 4 and FIG. 5, the support tube 180 is configuredto be sandwiched between the sheath 110 and the drive shaft 140 at thedistal side. As illustrated in FIG. 6, the support tube 180 isconfigured to be sandwiched between the inner shaft 130 and the driveshaft 140 at the proximal side.

As illustrated in FIG. 6, the support tube 180 is bonded to the innershaft 130 with adhesive B at the distal portion 130A of the inner shaft130. Accordingly, the support tube 180 is configured to be movableforward and backward in the axial direction in conjunction with theinner shaft 130.

As illustrated in FIG. 5, when the hub 160 is pulled toward the proximalside to a maximum extent (corresponding to the backward movement limitposition of the support tube 180), the support tube 180 is locatedcloser to the distal side than the injection opening 173 a. In otherwords, the injection opening 173 a is located closer to the proximalside than the distal end (a position indicated by reference character Bin FIG. 5) of the support tube 180 in the backward movement limitposition. According to this configuration, the priming liquid injectedvia the injection opening 173 a contacts the support tube 180 withoutdirectly contacting the drive shaft 140. Accordingly, the drive shaft140 can be prevented from deforming due to the priming liquid contactingthe drive shaft 140. Moreover, since the support tube 180 covers thedrive shaft 140 at the injection opening 173 a, when the drive shaft 140is rotated to acquire an image, the drive shaft 140 can be preventedfrom entering the injection opening 173 a and winding in a twisted orcontorted shape. The material used to configure the support tube 180 is,for example, a resin material.

It is desirable that, as illustrated in FIG. 5, the distal end of thesupport tube 180 in the backward movement limit position be locatedcloser to the injection opening 173 a. According to this configuration,the length in the axial direction of a portion forming a gap G betweenthe sheath 110 and the support tube 180 becomes small. Since the portionforming the gap G is a portion that is relatively high in flow pathresistance in the flow path through which the priming liquid flows, thelength of the gap G in the axial direction becoming small enablessmoothly performing the priming process.

As illustrated in FIG. 6, the unit connector 150 includes a unitconnector body 151, which is provided at the proximal side, and a covermember 152, which is provided at the distal side. The unit connector 150is equipped with a lumen 150 a, into which the inner shaft 130 and thedrive shaft 140 are inserted in such a way as to be movable forward andbackward.

A female screw portion 151A having a groove is provided on the internalsurface of the distal side of the unit connector body 151. A male screwportion 152A having a thread is provided on the external surface of theproximal side of the cover member 152. The unit connector body 151 isconfigured to be able to be attached to the cover member 152 by thefemale screw portion 151A of the unit connector body 151 being screwedon the male screw portion 152A of the cover member 152.

The outer tube 120 attached to the relay connector 170 is inserted intothe cover member 152, and the inner shaft 130 and the drive shaft 140,which extend from the hub 160, are inserted into the outer tube 120.

The material used to configure the unit connector body 151 and the covermember 152 can be a relatively hard resin material.

As illustrated in FIG. 7, the hub 160 includes a hub body 161, which hasa hollow shape, a connection pipe 164 b, which holds the drive shaft140, a sealing member 164 a, which seals a space between the hub body161 and the connection pipe 164 b, a bearing 164 c, which rotatablysupports the connection pipe 164 b, and a connector portion 165, insidewhich an electrode terminal 166 that is mechanically and electricallyconnectable to the external apparatus 300 is mounted.

The inner shaft 130 is connected to the distal portion of the hub 161.The drive shaft 140 is pulled out of the inner shaft 130 inside the hubbody 161.

The connection pipe 164 b holds the drive shaft 140 at the distal end ofthe connection pipe 164 b, which is an end portion opposite to a rotor167, so as to transmit the rotation of the rotor 167 to the drive shaft140. A seal member (not illustrated) is provided between the connectionpipe 164 b and the drive shaft 140. Therefore, the priming liquid can beprevented from flowing toward the proximal side and then contacting therotor 167.

The signal line 140 b (see FIG. 3) is inserted through the connectionpipe 164 b, and one end of the signal lime 140 b is connected to theelectrode terminal 166 and the other end thereof is connected to theultrasound transducer 145 a through the inside of the drive shaft 140. Areceived signal acquired by the ultrasound transducer 145 a istransmitted to the external apparatus 300 via the electrode terminal166, and is then subjected to predetermined processing to be displayedas an image.

The sealing member 164 a is, for example, an O-ring, and restrains thepriming liquid from moving toward the proximal side in the hub 160during the priming process. Therefore, the priming liquid can beprevented from flowing toward the proximal side and contacting the rotor167. Moreover, while air bubbles present in a lumen between theinjection opening 173 a and the sealing member 164 a move toward theproximal side due to a priming injection pressure applied when primingis performed, providing the sealing member 164 a prevents the airbubbles from moving toward the proximal side beyond the sealing member164 a.

Referring back to FIG. 1, the diagnostic imaging catheter 100 isconnected to and driven by the external apparatus 300.

As described above, the external apparatus 300 is connected to theconnector portion 165 (see FIG. 7) provided at the proximal side of thehub 160.

Furthermore, the external apparatus 300 includes a motor 300 a, which isa power source to rotate the drive shaft 140, and a motor 300 b, whichis a power source to move the drive shaft 140 in the axial direction.The rotational motion of the motor 300 b is converted into an axialmotion by a ball screw 300 c connected to the motor 300 b.

The operation of the external apparatus 300 is controlled by a controlapparatus 320 that is electrically connected to the external apparatus300. The control apparatus 320 includes a central processing unit (CPU)and a memory as main constituent elements. The control apparatus 320 iselectrically connected to a monitor 330.

Next, an example of using the diagnostic imaging catheter 100 accordingto the exemplary embodiment is described.

First, with the hub 160 pulled toward the proximal side to a maximumextent (see FIG. 2B and FIG. 5), the operator connects the syringe Sfilled with the priming liquid to the port 173, and the operator pushesthe plunger of the syringe S. In response to the plunger of the syringeS being pushed, the priming liquid is injected into the relay connector170 via the injection opening 173 a.

In the case of the diagnostic imaging catheter 100 according to theexemplary embodiment, since the injection opening 173 a is provided atthe relay connector 170, the length of the flow path through which thepriming liquid flows up to the communicating hole 116 is short ascompared with a configuration in which a port is provided at a unitconnector or a hub, and thus the flow path resistance is reduced.Moreover, since the support tube 180 is located closer to the distalside than the injection opening 173 a, the priming liquid injected viathe injection opening 173 a contacts the support tube 180 withoutdirectly contacting the drive shaft 140. Accordingly, the drive shaft140 can be prevented from deforming due to the force of the primingliquid impacting the drive shaft 140.

The priming liquid injected into the relay connector 170 flows towardthe distal side through the gap G between the sheath 110 and the supporttube 180 (see FIG. 5), and, after passing the distal end of the supporttube 180, flows toward the distal side through a gap between the sheath110 and the drive shaft 140 and is then injected into the lumen 110 a(see FIG. 3) of the sheath 110.

As the priming liquid is injected into the lumen 110 a, as illustratedin FIG. 3, the priming liquid is discharged to the outside of the sheath110 via the communicating passage 117 a and the communicating hole 116(see arrows in FIG. 3), so that a gas such as air can be discharged fromthe inside of the sheath 110 to the outside together with the primingliquid.

After the priming process, as illustrated in FIG. 1, the operatorconnects the external apparatus 300 to the connector portion 165 (seeFIG. 7) of the diagnostic imaging catheter 100. Then, the operatorpushes the hub 160 until the hub 160 contacts the proximal end of theunit connector 150 (see FIG. 2A), thus moving the transducer unit 145toward the distal side as illustrated in FIG. 3. In this state, thesheath 110 is inserted to a target position inside a body cavity (forexample, a blood vessel) along the guide wire W while the guide wire Wis inserted through the guide wire lumen 114 a.

To acquire a tomographic image at the target position inside the bodycavity, the transducer unit 145 is moved toward the proximal side (thepullback operation) while being rotated together with the drive shaft140. At this time, the ultrasound transducer 145 a of the transducerunit 145 transmits and receives ultrasound waves. Here, since thesupport tube 180 covers the drive shaft 140 at the injection opening 173a, the drive shaft 140 can be prevented from entering the injectionopening 173 a and winding in a twisted or contorted shape.

The rotation and movement operations of the drive shaft 140 arecontrolled by the control apparatus 320. The connector portion 165,which is provided inside the hub 160, is rotated in the state of beingconnected to the external apparatus 300, and the drive shaft 140 isrotated in conjunction with the connector portion 165. The rotationalspeed of the connector portion 165 and the drive shaft 140 is, forexample, 1,800 revolutions per minute (rpm).

Furthermore, the ultrasound transducer 145 a transmits ultrasound wavesinto the body based on a signal sent from the control apparatus 320. Asignal corresponding to ultrasound waves received by the ultrasoundtransducer 145 a is sent to the control apparatus 320 via the driveshaft 140 and the external apparatus 300. The control apparatus 320generates a tomographic image of the body cavity based on the signalsent from the ultrasound transducer 145 a, and displays the generatedimage on the monitor 330.

As described above, the diagnostic imaging catheter 100 according to theexemplary embodiment includes the drive shaft 140 which is provided withthe ultrasound transducer 145 a at a distal portion thereof and which isrotatable and movable forward and backward, the sheath 110 into whichthe drive shaft 140 is inserted, the relay connector 170 which iscoupled to a proximal end of the sheath 110, the support tube 180 whichis provided at an outer circumference of the drive shaft 140 along anaxial direction thereof and which moves forward and backward inconjunction with the drive shaft 140, the X-ring 175 which is providedinside the relay connector 170 and which seals a space between the relayconnector 170 and the support tube 180, and the injection opening 173 awhich is located in a region closer to a distal side than the X-ring 175and closer to a proximal side than a distal end (a position indicated byreference character B in FIG. 5) of the support tube 180 in a backwardmovement limit position thereof and via which a priming liquid is ableto be injected into the sheath 110. According to the diagnostic imagingcatheter 100 configured as mentioned above, the priming liquid isinjected via the injection opening 173 a, which is provided in a regioncloser to the distal side than the X-ring 175 provided inside the relayconnector 170. Therefore, the length of the flow path through which thepriming liquid flows up to the communicating hole 116 is short ascompared with a configuration in which a port is provided at a unitconnector or a hub, so that the flow path resistance is reduced.Accordingly, the flow path resistance is decreased without increasing agap between the sheath 110 and the drive shaft 140, so that the primingprocess can be smoothly performed. Moreover, since the injection opening173 a is located closer to the proximal side than the distal end (aposition indicated by reference character B in FIG. 5) of the supporttube 180 in the backward movement limit position, when the primingliquid is injected via the injection opening 173 a, the priming liquidcontacts the support tube 180 provided on the outer circumference of thedrive shaft 140. Accordingly, the priming liquid can be prevented fromcontacting the drive shaft 140 which can hinder appropriately acquiringan image. With the above-described configuration, the diagnostic imagingcatheter 100 can be provided which allows the priming process to besmoothly performed by reducing the flow path resistance withoutincreasing a gap between the sheath 110 and the drive shaft 140, whilepreventing the priming liquid from contacting the drive shaft 140 tohinder appropriately acquiring an image.

Furthermore, for example, in the case of a configuration in which a portis provided at a hub and a metallic pipe body in a sparsely wound coilshape is located between a drive shaft and an inner shaft, when thepriming liquid flows through the pipe body in the coil shape, airbubbles occur due to a difference in speed between the innercircumference and outer circumference of the pipe body. Then, the airbubbles may attach to the transducer unit 145 (air trap) as mentionedabove, so that an image may not be able to be appropriately acquired.However, in the case of the diagnostic imaging catheter 100 according tothe exemplary embodiment of the disclosure, since a pipe body in asparsely wound coil shape is not provided, the occurrence of the aboveair bubbles can be prevented. Accordingly, the occurrence of an air trapcan be prevented, and an image can be adequately acquired.

Moreover, the injection opening 173 a is provided at the relay connector170. According to this configuration, the length of the flow paththrough which the priming liquid flows up to the communicating hole 116is short as compared with a configuration in which a port is provided ata unit connector or a hub, so that the flow path resistance is reduced.Accordingly, the flow path resistance is decreased without increasing agap between the sheath 110 and the drive shaft 140, so that the primingprocess can be smoothly performed.

Additionally, in a case where the lesion area is, for example, aperipheral site such as a foot, since the length of the flow paththrough which the priming liquid flows is relatively large, providingthe injection opening 173 a at the relay connector 170, as in thediagnostic imaging catheter 100 according to the exemplary embodiment ofthe disclosure, enables more adequately reducing the flow pathresistance.

Further, the injection opening 173 a is located closer to the proximalside than the center of the relay connector 170. According to thisconfiguration, the injection opening 173 a is configured to be locatedcloser to the X-ring 175 in the axial direction than in a case where theinjection opening 173 a is located closer to the distal side than thecenter of the relay connector 170. Therefore, entrapment of air betweenthe injection opening 173 a and the X-ring 175 can be reduced.

Furthermore, the sealing member 164 a, which is provided inside the hub160 located on the proximal side of the relay connector 170 and operableto rotate and move the drive shaft 140 forward and backward, restrainsthe priming liquid and air (air bubbles) from moving toward the proximalside. According to this configuration, during the priming process, thepriming liquid can be prevented from flowing toward the proximal sideand contacting the rotor 167. Moreover, air bubbles present in a lumenbetween the injection opening 173 a and the sealing member 164 a can beprevented from moving toward the proximal side beyond the sealing member164 a.

Additionally, the port 173 which is coupled to the injection opening 173a is further included, and the port 173 is configured to be inclinedfrom the direction perpendicular to the axial direction toward theproximal side. According to this configuration, when the priming liquidis injected, the priming liquid is enabled to smoothly flow through theinjection opening 173 a toward the distal side, as compared with aconfiguration in which a port is provided along the directionperpendicular to the axial direction. Therefore, the force with whichthe operator pushes the syringe S can be decreased.

FIG. 8 is a diagram illustrating the entire configuration of adiagnostic imaging catheter 200 according to a further exemplaryembodiment of the disclosure here.

The diagnostic imaging catheter 200 according to the further exemplaryembodiment of the disclosure differs in the position where the syringe Sis connected from the diagnostic imaging catheter 100 according to theabove-described exemplary embodiment.

The diagnostic imaging catheter 200 according to the modificationexample 1 includes, as illustrated in FIG. 8, a sheath 110, an outertube 120, an inner shaft 130, a drive shaft 140, a relay connector 270,a support tube 180, a unit connector 150, and a hub 160. The sheath 110,the outer tube 120, the inner shaft 130, the drive shaft 140, thesupport tube 180, the unit connector 150, and the hub 160 haverespective configurations similar to those in the above-describedembodiment, and the description thereof is, therefore, omitted.

The relay connector 270 includes a port 273, which is coupled to theinjection opening 173 a through which the priming liquid is able to beinjected. A tube 274 extending toward the proximal side in the axialdirection is coupled to the port 273.

With the diagnostic imaging catheter 200 according to the furtherexemplary embodiment of the disclosure configured in this way, even in acase where it is difficult to connect the syringe S in the vicinity ofthe port 273, the priming liquid can be injected with the syringe Sconnected to the tube 274, which extends toward the proximal side.

While diagnostic imaging catheters according to the disclosure have beendescribed through the use of an exemplary embodiment and a furtherexemplary embodiment, the disclosure is not limited to only theconfigurations described in the exemplary embodiments, but can haveconfigurations that are changed or altered as appropriate based on theclaims.

For example, while, in the diagnostic imaging catheter 100 according tothe above-described exemplary embodiment, the injection opening 173 a isprovided at the relay connector 170, this is not so limiting as long asthe injection opening 173 a is provided in a region closer to the distalside than the X-ring 175.

Furthermore, while, in the diagnostic imaging catheter 100 according tothe above-described exemplary embodiment, the port 173 is formedintegrally with the outer tube holding portion 171, the port 173 can beformed integrally with the anti-kink protector 172. Additionally, theport 173 can be configured as a member separate from the anti-kinkprotector 172 or the outer tube holding portion 171.

Moreover, in the diagnostic imaging catheter 100 according to theabove-described exemplary embodiment, the injection opening 173 a islocated closer to the proximal side than the center of the relayconnector 170. However, the injection opening 173 a can be locatedcloser to the distal side than the center of the relay connector 170.

Furthermore, in the diagnostic imaging catheter 100 according to theabove-described exemplary embodiment, the port 173 is configured to beinclined from the direction perpendicular to the axial direction towardthe proximal side. However, the port 173 can be configured to extend inthe direction perpendicular to the axial direction.

Moreover, in the above-described exemplary embodiment, the primingliquid is injected into the relay connector 170 by the operator pushingthe plunger of the syringe S. However, the priming liquid can beinjected into the relay connector 170 by the plunger of the syringe Sbeing pushed by a mechanical configuration and operation.

Additionally, while, in the above-described exemplary embodiment, adiagnostic imaging catheter for use in intravascular ultrasound (IVUS)is taken as an example of an application target for a diagnostic imagingcatheter according to the disclosure, the disclosure herein can also beapplied to, for example, a diagnostic imaging catheter for use inoptical coherence tomography (OCT) and a hybrid-type (dual-type)diagnostic imaging catheter usable in both intravascular ultrasound andoptical coherence tomography.

The detailed description above describes features and aspects of anembodiment of a diagnostic imaging catheter. The invention is notlimited, however, to the precise embodiment and variations described.Various changes, modifications and equivalents could be effected by oneskilled in the art without departing from the spirit and scope of theinvention as defined in the appended claims. It is expressly intendedthat all such changes, modifications and equivalents which fall withinthe scope of the claims are embraced by the claims.

What is claimed is:
 1. A diagnostic imaging catheter comprising: asheath; a drive shaft provided with a signal transmitting and receivingunit at a distal portion thereof, which is configured to be insertedinto the sheath, and which is rotatable and movable forward and backwardrelative to the sheath; a relay connector coupled to a proximal end ofthe sheath; a support tube provided at an outer circumference of thedrive shaft along an axial direction and which moves forward andbackward in conjunction with the drive shaft; a seal member providedinside the relay connector and which seals a space between the relayconnector and the support tube; and an injection opening which islocated in a region closer to a distal side of the catheter than theseal member and closer to a proximal side of the catheter than a distalend of the support tube when the support tube is in a backward movementlimit position and via which a liquid is able to be injected into thesheath.
 2. The diagnostic imaging catheter according to claim 1, whereinthe injection opening is provided in the relay connector.
 3. Thediagnostic imaging catheter according to claim 2, wherein the injectionopening is located closer to the proximal side than a center of therelay connector in the axial direction.
 4. The diagnostic imagingcatheter according to claim 1, further comprising a sealing member whichis provided inside a hub located on a proximal side of the relayconnector and operable to rotate and move the drive shaft forward andbackward and which restrains the liquid from moving toward the proximalside of the catheter.
 5. The diagnostic imaging catheter according toclaim 1, further comprising a port which communicates with the injectionopening, wherein the port is configured to be inclined from a directionperpendicular to the axial direction toward the proximal side of thecatheter.
 6. The diagnostic imaging catheter according to claim 5,further comprising a tube which communicates with the injection openingvia the port and which extends along the axial direction.
 7. Thediagnostic imaging catheter according to claim 5, wherein the port isintegrally formed with the relay connector.
 8. The diagnostic imagingcatheter according to claim 1, further comprising an outer tube providedat a proximal side of the sheath, the relay connector interconnectingthe sheath and the outer tube.
 9. The diagnostic imaging catheteraccording to claim 8, wherein the relay connector includes an outer tubeholding portion provided on a proximal side of the relay connector andan anti-kink protector provided on a distal side of the relay connector.10. The diagnostic imaging catheter according to claim 9, wherein theseal member seals a space between the outer tube holding portion and thesupport tube.
 11. A diagnostic imaging catheter comprising: a sheathincluding a lumen; a drive shaft including a signal transmitting andreceiving unit at a distal portion thereof, the drive shaft configuredto be inserted in the lumen of the sheath and be rotatable and movableforward and backward relative to the sheath; a relay connector coupledto a proximal end of the sheath; a support tube provided around an outercircumference of the drive shaft along an axial direction, the supporttube being movable forward and backward in conjunction with the driveshaft from a forward movement limit position to a backward movementlimit position; a seal member provided inside the relay connector, theseal member configured to seal a space between the relay connector andthe support tube; and an injection opening configured for fluid to beinjected therethrough and into the sheath, wherein, when the supporttube is in the backward movement limit position, the injection openingis located closer to a distal side of the catheter than the seal memberand closer to a proximal side of the catheter than a distal end of thesupport tube, whereby fluid injected through the injection openingcontacts the support tube provided around the outer circumference of thedrive shaft rather than directly contacting the drive shaft.
 12. Thediagnostic imaging catheter according to claim 11, wherein the sealmember comprises an X-ring.
 13. The diagnostic imaging catheteraccording to claim 11, further comprising a hub located on a proximalside of the relay connector and operable to rotate and move the driveshaft forward and backward.
 14. The diagnostic imaging catheteraccording to claim 11, wherein the sheath includes a discharge holeformed at a distal portion thereof such that fluid injected into thesheath through the injection opening can be discharged from the sheathvia the discharge hole.
 15. The diagnostic imaging catheter according toclaim 11, further comprising a port configured to communicate with theinjection opening, the port being inclined from a directionperpendicular to the axial direction toward the proximal side of thecatheter.
 16. The diagnostic imaging catheter according to claim 15,wherein the port is integrally formed with the relay connector.
 17. Amethod of using a diagnostic imaging catheter comprising the steps of:providing a diagnostic imaging catheter including a sheath including alumen; a drive shaft including a transducer unit at a distal portionthereof, the drive shaft configured to be inserted in the lumen of thesheath and be rotatable and movable forward and backward relative to thesheath; a relay connector coupled to a proximal end of the sheath; asupport tube provided around an outer circumference of the drive shaftalong an axial direction, the support tube being movable forward andbackward in conjunction with the drive shaft from a forward movementlimit position to a backward movement limit position; an injectionopening configured for fluid to be injected therethrough and into thesheath; a port which communicates with the injection opening; and a hublocated on a proximal side of the relay connector and operable to rotateand move the drive shaft forward and backward; pulling the hub toward aproximal side of the catheter to a maximum extent; connecting a syringefilled with a fluid to the port; pushing a plunger of the syringe suchthat the fluid is injected into the relay connector via the injectionopening; discharging the fluid outside of the sheath via a dischargehole in the sheath; connecting a connector portion of the diagnosticimaging catheter to an external apparatus; pushing the hub toward adistal side of the catheter to a maximum extent and moving thetransducer unit toward a distal side of the sheath; inserting the sheathto a target position inside a body cavity; acquiring a tomographic imageat the target position by moving the transducer unit toward the proximalside of the catheter in a pullback operation while being rotatedtogether with the drive shaft; wherein the drive shaft is covered by thesupport tube at the injection opening during the pullback operation,thereby preventing the drive shaft from entering the injection opening;wherein the diagnostic imaging catheter further comprises a seal memberprovided inside the relay connector, the seal member configured to seala space between the relay connector and the support tube; and wherein,when the support tube is in the backward movement limit position, theinjection opening is located closer to a distal side of the catheterthan the seal member and closer to a proximal side of the catheter thana distal end of the support tube, wherein the fluid injected through theinjection opening contacts the support tube provided around the outercircumference of the drive shaft rather than directly contacting thedrive shaft.
 18. The method of using a diagnostic imaging catheteraccording to claim 17, wherein the external apparatus utilizesintravascular ultrasound.
 19. The method of using a diagnostic imagingcatheter according to claim 17, further comprising providing the port atan incline toward the proximal side of the catheter from a directionperpendicular to the axial direction.